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WO1993015608A1 - Facteurs specifiques prevenant les lesions et la degenerescence retinales - Google Patents

Facteurs specifiques prevenant les lesions et la degenerescence retinales Download PDF

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Publication number
WO1993015608A1
WO1993015608A1 PCT/US1993/001328 US9301328W WO9315608A1 WO 1993015608 A1 WO1993015608 A1 WO 1993015608A1 US 9301328 W US9301328 W US 9301328W WO 9315608 A1 WO9315608 A1 WO 9315608A1
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Prior art keywords
retinal
factor
administration
mammal
degeneration
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PCT/US1993/001328
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English (en)
Inventor
Matthew M. Lavail
Roy H. Steinberg
George D. Yancopolous
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Regeneron Pharmaceuticals, Inc.
The Regents Of The University Of California
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Publication date
Application filed by Regeneron Pharmaceuticals, Inc., The Regents Of The University Of California filed Critical Regeneron Pharmaceuticals, Inc.
Priority to CA002130115A priority Critical patent/CA2130115C/fr
Priority to AU36194/93A priority patent/AU677951B2/en
Priority to EP93905054A priority patent/EP0671879B1/fr
Priority to DE69328730T priority patent/DE69328730T2/de
Priority to JP51432493A priority patent/JP3645902B2/ja
Priority to AT93905054T priority patent/ATE193207T1/de
Publication of WO1993015608A1 publication Critical patent/WO1993015608A1/fr
Priority to HK98109177A priority patent/HK1008292A1/xx

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/19—Cytokines; Lymphokines; Interferons
    • A61K38/20—Interleukins [IL]
    • A61K38/2006—IL-1
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/18—Growth factors; Growth regulators
    • A61K38/1825—Fibroblast growth factor [FGF]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/18—Growth factors; Growth regulators
    • A61K38/185—Nerve growth factor [NGF]; Brain derived neurotrophic factor [BDNF]; Ciliary neurotrophic factor [CNTF]; Glial derived neurotrophic factor [GDNF]; Neurotrophins, e.g. NT-3
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/19—Cytokines; Lymphokines; Interferons
    • A61K38/191—Tumor necrosis factors [TNF], e.g. lymphotoxin [LT], i.e. TNF-beta
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides
    • A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • A61K38/17—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • A61K38/19—Cytokines; Lymphokines; Interferons
    • A61K38/20—Interleukins [IL]
    • A61K38/2093—Leukaemia inhibitory factor [LIF]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0048—Eye, e.g. artificial tears
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV

Definitions

  • the present invention relates to a method of preventing or delaying retinal degeneration caused by exposure to light or other environmental trauma, or by any pathological condition wherein death or injury of retinal neurons or photoreceptors occurs. It is based on the discovery that specific survival promoting factors, when introduced into the living mammalian eye, prevent damage and degeneration of photoreceptors caused by light and on the further discovery that such factors can delay photoreceptor degeneration associated with inherited diseases of the retina.
  • Trophic factors play a major role in neuronal survival and growth during development, in addition to the maintenance of differentiated neurons. Such factors also appear to play a role in the survival and regeneration of injured neurons in the central as well as in the peripheral nervous system.
  • a number of diseases of the retina involve injury or degeneration of retina-associated neurons.
  • Trophic factors capable of rescuing these neurons may provide useful therapies for the treatment of such diseases.
  • NGF neurotrophic factor
  • BDNF brain derived neurotrophic factor
  • retinal ganglion cells could be maintained by extracts from the neonatal superior colliculus and that a factor purified from such " extracts promotes the survival and growth of retinal ganglion cells in vivo. (Schultz, et al. ⁇ .
  • fibroblast growth factors promote the survival of adult rat ganglion cells after application to transected optic nerves (Sievers, et al., Neurosci. Let. 76 (1987):157-162).
  • Photoreceptors consist of rods and cones which are the photosensitive cells of the retina.
  • the rods contain rhodopsin, the rod photopigment, and the cones contain 3 distinct photopigments, which
  • SUBSTI respond to light and ultimately trigger a neural discharge in the output cells of the retina, the ganglion cells. Ultimately, this signal is registered as a visual stimulus in the visual cortex.
  • the retinal pigment epithelial (RPE) cells produce, store and transport a variety of factors that are responsible for the normal function and survival of photoreceptors.
  • RPE are multifunctional cells that transport metabolites to the photoreceptors from their blood supply, the chorio capillaris of the eye.
  • the RPE cells also function to recycle vitamin A as it moves between the photoreceptors and the RPE during light and dark adaptation.
  • RPE cells also function as macrophages, phagocytizmg the rhythmically-shed tips of the outer segments of rods and cones.
  • Various ions, proteins and water move between the RPE cells and the interphotoreceptor space, and these molecules ultimately effect the metabolism and viability of the photoreceptors.
  • RCS Royal College of Surgeons
  • RCS Royal College of Surgeons
  • RCS Reyal College of Surgeons
  • bFGF is unable to remedy one particular defect seen in RCS rats, which is the inability of the RPE to phagocytosize degenerated neurons.
  • results obtained using such rats as a model to identify survival enhancing factors appear to correlate well with data obtained using RCS rats. Moreover, different factors can be compared and complications can be assessed more quickly in the light damage model than can be assessed by testing factors in models which are
  • An object of the present invention is to provide a method of preventing injury or death of retinal neurons.
  • Another object of the invention is to provide a method of treating pathological diseases wherein degeneration of the retina occurs.
  • Yet another object of the invention is to provide a method of treating the living eye prior to or following exposure to light or other environmental trauma thereby preventing degeneration of retinal cells.
  • a further object of the present invention is to provide a method of preventing photoreceptor injury and degeneration in the living eye.
  • SUBSTITUTE SHEET Another object of the invention is to provide an in vivo assay system for assessing the survival-promoting activity of neurotrophic and other cellular factors on retinal neurons and photoreceptors.
  • a neurotrophic factor such as brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), neurotrophin-3 (NT-3) or neurotrophin-4 (NT-4), or a cellular factor such as acidic fibroblast growth factor (aFGF), basic fibroblast growth factor (bFGF) plus heparin, aFGF plus heparin, interleukin-1 beta (IL-l ⁇ ), tumor necrosis factor-alpha (TNF- ⁇ ) and insulin-like growth factor-2 (IGF-2).
  • BDNF brain-derived neurotrophic factor
  • CNTF ciliary neurotrophic factor
  • NT-3 neurotrophin-3
  • NT-4 neurotrophin-4
  • a cellular factor such as acidic fibroblast growth factor (aFGF), basic fibroblast growth factor (bFGF) plus heparin, aFGF plus heparin, interleukin-1 beta (IL-l ⁇ ), tumor necrosis factor-alpha (TNF- ⁇ ) and insulin-like growth factor
  • FIG. 1 is a histogram illustrating the degree of photoreceptor rescue obtained using the neurotrophic and cellular factors.
  • FIG. 2 is a histogram illustrating the ONL thickness obtained using the neurotrophic and cellular factors.
  • FIG. 3 is a composite of three light micrographs showing a) control retina from a rat not exposed to light; b) control retina from a rat exposed to light after PBS injection; and c) BDNF-treated rat retina after exposure to light.
  • FIG. 4 is a histogram illustrating the degree of macrophage incidence observed using the neurotrophic and cellular factors.
  • the present invention provides for the utilization of neurotrophic, as well as other cellular factors to delay, prevent or rescue photoreceptors, as well as other retinal cells, including neurons or supportive cells (e.g. Muller cells or RPE cells) from injury and degeneration.
  • Other retinal neurons include, but are not limited to, retinal ganglion cells, displaced retinal ganglion cells, amacrine cells, displaced amacri ⁇ e cells, horizontal and bipolar neurons.
  • neurotrophic or other cellular factors are utilized to treat any condition which results in injury or death of photoreceptors or other retinal cells.
  • conditions include: retinal detachment; age-related and other maculopathies, photic retinopathies; surgery-induced retinopathies (either mechanically or light-induced); toxic retinopathies including those resulting from foreign bodies in the eye; diabetic retinopathies; retinopathy of prematurity; viral retinopathies such as CMV or HIV retinopathy related to AIDS; uveitis; ischemic retinopathies due to venous or arterial occlusion or other vascular disorders; retinopathies due to trauma or penetrating lesions of the eye; peripheral vitreoretinopathy; and inherited retinal degenerations.
  • the factors which are useful in practicing this invention include one or more neurotrophic factor such as brain-derived neurotrophic factor (BDNF), ciliary neurotrophic factor (CNTF), neurotrophin-3 (NT-3), neurotrophm-4
  • BDNF brain-derived neurotrophic factor
  • CNTF ciliary neurotrophic factor
  • NT-3 neurotrophin-3
  • neurotrophm-4 neurotrophic factor
  • NT-4 or functional derivatives or analogs thereof, or one or more cellular factor such as basic fibroblast growth factor (bFGF) plus heparin, acidic fibroblast growth factor (aFGF), aFGF plus heparin, leukemia inhibitory - factor (LIF), interleukin-1 beta (IL-l ⁇ ), tumor necrosis factor-alpha (TNF- ⁇ ), and insulin-like growth factor-2 (IGF-2), or functional derivatives or analogs thereof.
  • Other factors that appears to be effective, but to a lesser extent, include nerve growth factor (NGF), heparin, epidermal growth factor (EGF), platelet derived growth factor (PDGF) and insulin-like growth factor-1 (IGF- 1).
  • a functional derivative of a factor is a compound which is an analog or an active fragment of the compound or its analog. Combinations of the neurotrophic factors and cellular factors may also be used to achieve optimum results.
  • Each of the factors utilized may be obtained by methods known by those skilled in the art. For example, they may be purified from a natural source. Alternatively, they may be made by recombinant means utilising; available sequence data. (See, for example, for CNTF; Masiakowski, et al. J. Neurochemistry 57(1991): 1003-1012; NT-3; Maisonpierre, et al. Science 247(1990): 1446-1451).
  • a recombinant bacteriophage (HG7-2), containing a human genomic sequence related to neurotrophin-4 was deposited on - August 22, 1991 with the American Type Culture Collection, 12301 Parklawn Drive, Rockville, Maryland 20852, and assigned accession number ATCC 75070.
  • neurotrophic factors are proteins responsible for the development and maintenance of the nervous system. Widespread neuronal cell death accompanies normal development of the
  • neuronal cell death results from the competition among neurons for limiting amounts of survival factors ("neurotrophic factors")-
  • the important neurotrophic factors identified to date are NGF, BDNF, CNTF, NT-3 and NT-4.
  • BDNF is utilized to treat any condition which results in injury or death of photoreceptors or other retina-related cells.
  • molecular cloning of BDNF, as well as the resultant production and purification of purified recombinant BDNF, as described in USSN 400,591 it became possible to determine the physiological effects of BDNF on developing neurons, as well as to quantify the levels of BDNF in tissues by immunoassay and to localize BDNF in tissues using immunocytochemistry.
  • a BDNF cDNA was found in a retinal library and BDNF mRNA was found to be expressed in adult retinas (Maisonpierre, et al.
  • ciliary neurotrophic factor is used to prevent or delay photoreceptor degeneration.
  • CNTF like BDNF, effectively protects photoreceptors without macrophage influx and the mitogenic and angiogenic properties of bFGF.
  • NT-4 is used to prevent photoreceptor degeneration. As with BDNF and CNTF, NT-4 effectively protects photoreceptors without macrophage influx or any mitogenic or angiogenic effects.
  • lleukemia inhibitory factor (LIF) is used to prevent photoreceptors from injury.
  • aFGF is used to prevent photoreceptor degeneration. This factor, unlike bFGF, appears to provide protection without the influx of macrophages observed when bFGF is used.
  • bFGF is used in conjunction with a compound that suppresses the influx of macrophages observed using bFGF alone. Heparin appears to be useful for this purpose. Combinations of heparin and bFGF prevent photoreceptor injury without macrophage influx, and heparin enhances the action of aFGF, as well as bFGF (see Figure 4).
  • IL-l ⁇ and TNF- ⁇ provide a substantial amount of retinal protection.
  • IL-l ⁇ however, has been observed to cause folding and rosette formation and a somewhat greater incidence of macrophages than is observed in control retinas or those protected with BDNF or CNTF.
  • Use of TNF- ⁇ may also be associated with a slightly greater than normal incidence of macrophages.
  • the light damage model may be used to evaluate the effect of various survival-promoting factors on the retina.
  • the intravitreal administration of various factors into the eves of albino rats enabled the rapid assessment of both the ability of the factors to rescue photoreceptors from degeneration and the side effects, such as incidence of macrophages, associated with each factor.
  • the model described herein is the albino rat, the eyes of other albino mammals, such as mice and rabbits, are also useful for this purpose.
  • the light damage model has been used previously to assess the effect of various agents such as antioxidents on the retina, such studies have always been conducted using systemic (intraperitoneal) administration.
  • systemic intraperitoneal
  • the intravitreal injection of potential survival promoting factors represents a novel method of assessing factors, with several advantages over systemic application.
  • the amount of any specific agent that reaches the retina can be more accurately determined, since the eye is a round, relatively contained structure and the agent is injected directly into it.
  • the amoimt of agent that need to be injected is minuscule compared to systemic injections.
  • a single microliter in volume (about 1 rr ⁇ crogram of agent) is used for intravitreal injection, as compared to one to several milliliters (ten to several hundred milligrams of agent) necessary for systemic injections.
  • the intravitreal route of administration avoids the potentially toxic effect of some agents.
  • the factors used herein prevent the degeneration of retinal cells. It has been further observed that when animals that have been exposed to damaging light are returned to normal light, they will regenerate their inner and outer segments. Thus, :..e factors of the present invention are able not only to protect and prevent photoreceptors from degeneration, but also to promote regeneration of retinal cells.
  • the factors of the present invention can be delivered to the eye through a variety of routes. They may be delivered intraocularly, by topical application to the eye or by intraocular injection into, for example the vitreous or subretinal (interphotoreceptor) space. Alternatively, they may be delivered locally by insertion or injection into the tissue surrounding the eve. They may be delivered systemically through an oral route or by subcutaneous, intravenous or intramuscular injection. Alternatively, they may be delivered by means of a catheter or by means of an implant, wherein such an implant is made of a porous, non-porous or gelatinous material, including membranes such as silastic membranes or fibers, biodegradable . polymers, or proteinaceous material.
  • the factors may be administered prior to the onset of the condition, to prevent its occurrence, for example, during surgery on the eye, or immediately after the onset of the pathological condition or during the occurrence of an acute or protracted condition.
  • the factors of the present invention may be modified to enhance their ability to penetrate the blood-retinal barrier. Such modifications may include increasing their lipophilicity by, for example, glycosylation, or increasing their net charge by methods known in the art.
  • the factors may be delivered alone or in combination, and may be delivered along with a pharmaceutically acceptable vehicle. Ideally, such a vehicle would enhance the stability and/or delivery properties.
  • the invention also provides for pharmaceutical compositions containing the active factor or fragment or derivative thereof, which can be administered using a suitable vehicle such as liposomes, micro par tides or microcapsules. In various embodiments of the invention, it may be useful to use such compositions to achieve sustained release of the active component.
  • Albino rats of either the F344 or Sprague-Dawley strain were used at 2-5 months of age.
  • the rats were maintained in a cyclic tight environment (12 hr on: 12 hr off at an in-cage illuminance of less than 25 ft-c) for 9 or more days before being exposed to constant light.
  • the rats were exposed to 1 or 2 weeks of constant light at an illuminance level of 115-200 ft-c (most rats received 125-170 ft-c) provided by two 40 watt General Electric "cool-white" fluorescent bulbs with a white reflector that was suspended 60cm above the floor of the cage.
  • rats were maintained in transparent polycarbonate cages with stainless steel wire-bar covers.
  • rats anesthetized with a ketamine-xylazine mixture were injected intravitreally with 1 ⁇ l of the various factors dissolved in phosphate buffered saline (PBS) at a concentration of 50-1000 ng/ ⁇ l.
  • PBS phosphate buffered saline
  • the injections were made with the insertion of a 32 gauge needle through the sclera, choroid and retina approximately midway between the ora serrata and equator of the eye.
  • the factor-injected animals were compared to either uninjected littermates or to those that received intravitreal injections of 1 ⁇ l of PBS alone, as well as to animals that were not exposed to constant light. Controls included the injection of 1 ⁇ l of PBS alone, or the
  • the rats were killed by ' overdose of carbon dioxide followed immediately by vascular perfusion of mixed aldehydes.
  • the eyes were embedded in epoxy resin for sectioning at 1 ⁇ m thickness to provide sections of the entire retina along the vertical meridian of the eye.
  • the degree of light-induced retinal degeneration was quantified by two methods. The first was by measuring outer nuclear layer (ONL) thickness, which is used as an index of photoreceptor cell loss.
  • ONL thickness was obtained from a single section of each animal with the aid of a Bioquant morphometry system. In each of the superior and inferior hemispheres, ONL thickness was measured in 9 sets of 3 measurements each (total of 27 measurements in each hemisphere).
  • Each set was centered on adjacent 440- ⁇ m lengths of retina (the diameter of the microscope field at 400X magnification).
  • the first set of measurements was taken at approximately 440 ⁇ m from the optic nerve head, and subsequent sets were located more peripherally.
  • the 3 measurements were made at defined points separated from one another by 75 ⁇ m using an eyepiece micrometer. In this way, the 54 measurements in the two hemispheres sampled representative regions of almost the entire retinal section.
  • Figure 1 The results obtained with each of the factors tested are summarized in Figure 1.
  • the second method of assessing the degree of photoreceptor rescue was by a 0-4+ pathologist's scale of rescue, 4+ being maximal rescue and almost normal retinal integrity.
  • Neurotrophic factors BDNF, NT-4 and CNTF provided a high degree of rescue.
  • the factors LIF, bFGF, aFGF, bFGF plus heparin, aFGF plus heparin, TNF- ⁇ , IL-l ⁇ , NT-3 and IGF-2 also provided a significant amount of rescue.
  • all of the factors other than bFGF enhanced survival without inducing a high incidence of macrophages, as seen in Figure 4 (IL-l ⁇ and TNF- ⁇ were associated with a slightly higher incidence of macrophages).
  • Acidic fibroblast growth factor (aFGF), which had previously been reported to be ineffective as compared to bFGF in the RCS rat, was shown to provide significant protection of photoreceptors in the light-damage model.
  • aFGF Acidic fibroblast growth factor

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Abstract

On évite des lésions ou la mort de cellules photoréceptrices (dégérescence rétinienne) en introduisant dans l'oeil des mammifères des facteurs spécifiques de promotion de survie qui préviennent les dommages et la dégénérescence des photorécepteurs avant, pendant ou après leur exposition aux effets nuisibles de la lumière. Ces facteurs retardent également l'apparition des dommages provenant de maladies héréditaires.
PCT/US1993/001328 1992-02-14 1993-02-12 Facteurs specifiques prevenant les lesions et la degenerescence retinales WO1993015608A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002130115A CA2130115C (fr) 1992-02-14 1993-02-12 Prevention des lesions et des degenerescences retiniennes par des facteurs specifiques
AU36194/93A AU677951B2 (en) 1992-02-14 1993-02-12 Prevention of retinal injury and degeneration by specific factors
EP93905054A EP0671879B1 (fr) 1992-02-14 1993-02-12 Prevention des lesions et de la degenerescence des photorecepteurs par des facteurs neurotrophiques
DE69328730T DE69328730T2 (de) 1992-02-14 1993-02-12 Vorbeugung von verletzungen und degenerationen von photorezeptoren durch neurotrophische faktoren
JP51432493A JP3645902B2 (ja) 1992-02-14 1993-02-12 特定の因子による網膜の損傷および変性の防止
AT93905054T ATE193207T1 (de) 1992-02-14 1993-02-12 Vorbeugung von verletzungen und degenerationen von photorezeptoren durch neurotrophische faktoren
HK98109177A HK1008292A1 (en) 1992-02-14 1998-07-15 Prevention of injury and degeneration of photoreceptors by neurotrophic factors

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US83609092A 1992-02-14 1992-02-14
US836,090 1992-02-14
US89730792A 1992-06-11 1992-06-11
US897,307 1992-06-11

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JP (1) JP3645902B2 (fr)
CN (1) CN1077799C (fr)
AT (1) ATE193207T1 (fr)
AU (1) AU677951B2 (fr)
CA (1) CA2130115C (fr)
DE (1) DE69328730T2 (fr)
HK (1) HK1008292A1 (fr)
IL (1) IL104726A (fr)
WO (1) WO1993015608A1 (fr)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5441937A (en) * 1988-10-31 1995-08-15 Houston Biotechnology Incorporated Neurotrophic factor
WO1997019694A1 (fr) * 1995-11-29 1997-06-05 Amgen Inc. Procedes de traitement de photorecepteurs a l'aide d'un produit proteique de type facteur neurotrophique derive de lignee cellulaire gliale (gdnf)
US5641749A (en) * 1995-11-29 1997-06-24 Amgen Inc. Method for treating retinal ganglion cell injury using glial cell line-derived neurothrophic factor (GDNF) protein product
EP0820467A1 (fr) * 1995-03-27 1998-01-28 Cambridge Neuroscience, Inc. Procedes de traitement de troubles oculaires
WO1998050065A2 (fr) * 1997-05-05 1998-11-12 Marion Sangster Eckmiller Utilisation de principes actifs a effet biologique pour influer sur l'espace extracellulaire de cellules sensorielles et procede de commande d'administration de principe actif et dispositif approprie
US5843893A (en) * 1992-02-19 1998-12-01 Pharmacia S.P.A. Method for inhibiting the proliferation of epithelial lens cells and implantable lens therefor
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Cited By (14)

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US5441937A (en) * 1988-10-31 1995-08-15 Houston Biotechnology Incorporated Neurotrophic factor
US6780837B1 (en) 1989-08-30 2004-08-24 The Regents Of The University Of California Prevention of retinal injury and degeneration by specific factors
US5843893A (en) * 1992-02-19 1998-12-01 Pharmacia S.P.A. Method for inhibiting the proliferation of epithelial lens cells and implantable lens therefor
JP2008133285A (ja) * 1993-08-12 2008-06-12 Neurotech Usa Inc 遺伝的に改変された細胞を含む生体適合性免疫隔離カプセル
EP0820467A4 (fr) * 1995-03-27 2001-12-05 Cambridge Neuroscience Inc Procedes de traitement de troubles oculaires
EP0820467A1 (fr) * 1995-03-27 1998-01-28 Cambridge Neuroscience, Inc. Procedes de traitement de troubles oculaires
US6750196B1 (en) 1995-03-27 2004-06-15 Acorda Therapeutics Methods of treating disorders of the eye
US5641750A (en) * 1995-11-29 1997-06-24 Amgen Inc. Methods for treating photoreceptors using glial cell line-derived neurotrophic factor (GDNF) protein product
US5641749A (en) * 1995-11-29 1997-06-24 Amgen Inc. Method for treating retinal ganglion cell injury using glial cell line-derived neurothrophic factor (GDNF) protein product
WO1997019694A1 (fr) * 1995-11-29 1997-06-05 Amgen Inc. Procedes de traitement de photorecepteurs a l'aide d'un produit proteique de type facteur neurotrophique derive de lignee cellulaire gliale (gdnf)
WO1998050065A3 (fr) * 1997-05-05 1999-06-10 Marion Sangster Eckmiller Utilisation de principes actifs a effet biologique pour influer sur l'espace extracellulaire de cellules sensorielles et procede de commande d'administration de principe actif et dispositif approprie
WO1998050065A2 (fr) * 1997-05-05 1998-11-12 Marion Sangster Eckmiller Utilisation de principes actifs a effet biologique pour influer sur l'espace extracellulaire de cellules sensorielles et procede de commande d'administration de principe actif et dispositif approprie
EP1179020A1 (fr) * 1999-05-06 2002-02-13 The Schepens Eye Research Institute, Inc. Recuperation de cellules photoreceptrices induite par il-1beta administree a faible dose et ne provoquant pas de dysplasie retinienne
EP1179020A4 (fr) * 1999-05-06 2004-08-18 Schepens Eye Res Inst Recuperation de cellules photoreceptrices induite par il-1beta administree a faible dose et ne provoquant pas de dysplasie retinienne

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EP0671879A1 (fr) 1995-09-20
CA2130115A1 (fr) 1993-08-19
ATE193207T1 (de) 2000-06-15
CN1080188A (zh) 1994-01-05
IL104726A0 (en) 1993-06-10
EP0671879A4 (fr) 1996-01-17
DE69328730D1 (de) 2000-06-29
IL104726A (en) 2000-07-26
AU3619493A (en) 1993-09-03
DE69328730T2 (de) 2000-09-28
EP0671879B1 (fr) 2000-05-24
CN1077799C (zh) 2002-01-16
HK1008292A1 (en) 1999-05-07
JP3645902B2 (ja) 2005-05-11
JPH07507053A (ja) 1995-08-03
AU677951B2 (en) 1997-05-15
CA2130115C (fr) 2004-09-14

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